HSPA5 heat shock protein family A (Hsp70) member 5
Information
- Symbol
- HSPA5
- Type
- protein-coding
- Description
- heat shock protein family A (Hsp70) member 5
- Entrez Gene ID
- 3309
- Genome
- hg19
- Position
- chr9:127,997,132-128,003,622
- Genome
- hg38
- Position
- chr9:125,234,853-125,241,343
- MIM
- 138120 OMIM
- HGNC
- HGNC:5238 HGNC
- Ensembl
- ENSG00000044574 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely pathogenic | 1 | 0 |
| Benign | 0 | 6 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| Category | : |
|
| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | BIP |
| SYNONYM | GRP78 |
| SYNONYM | HEL-S-89n |
| MIM | 138120 OMIM |
| HGNC | HGNC:5238 HGNC |
| Ensembl | ENSG00000044574 Ensembl |
| AllianceGenome | HGNC:5238 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000680272.1 | hg38 | chr9 | 125,234,860 | 125,241,368 | 6,509 |
| ENST00000680032.1 | hg38 | chr9 | 125,236,489 | 125,241,382 | 4,894 |
| ENST00000324460.7 | hg38 | chr9 | 125,234,853 | 125,241,343 | 6,491 |
| ENST00000324460.7 | hg19 | chr9 | 127,997,132 | 128,003,622 | 6,491 |
| ENST00000680272.1 | hg19 | chr9 | 127,997,139 | 128,003,647 | 6,509 |
| ENST00000680032.1 | hg19 | chr9 | 127,998,768 | 128,003,661 | 4,894 |
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